NDC 10107-431-01 - Herb Street Arthritis Relief
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 10107-431
- Requested NDC
- 10107-431-01
- Package NDCs from labels
- 10107-431-01, 10107-431-02
- Manufacturer
- Balassa Laboratories Inc.
- Effective date
- 2024-10-01
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Herb Street Arthritis Relief | Balassa Laboratories Inc. | 2024-10-01 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 10107-431-01 | Herb Street Arthritis Relief | 16.8 g in 1 TUBE | STICK | 16.8 | 2 | |
| 10107-431-02 | Herb Street Arthritis Relief | 1 in 1 CARTON | STICK | 1 | 2 |
DailyMed Dashboard NDC Coverage#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.